ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C
Reason for recall
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C, (6) G5A-13C, (7) G5A-15C, (8) G5A-22C, (9) G5A-41C, (10) G5A-85C, (11) G5A-90C (12) G5A-80-L; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). There are two models available fully automatic and semi-automatic. After the defibrillations pads are applied to the patient, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is detected, delivers a shock without any rescuer assistance. The semi-automatic model evaluates the heart rhythm and requires the rescuer to press the shock button if a shockable rhythm is detected. Both models have voice and text instructions that guide the rescuer through the entire defibrillation process. Note: Not all configurations described in this document are available in all areas.
Lot / code information
- Catalog #
- (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C, (6) G5A-13C, (7) G5A-15C, (8) G5A-22C, (9) G5A-41C, (10) G5A-85C, (11) G5A-90C (12) G5A-80-L
- UDI
- (1) 00812394021161, (2) no
- UDI
- , (3) no
- UDI
- , (4) no
- UDI
- , (5) no
- UDI
- , (6) no
- UDI
- , (7) no
- UDI
- , (8) no
- UDI
- , (9) no
- UDI
- , (10) 00812394021208 (11) no
- UDI
- , (12) 00812394021215
- Serial #
(1) D00000066618, D00000066630, D00000066659, D00000066773, D00000067078, D00000067079 — +954 moreShow all
(1) D00000066618, D00000066630, D00000066659, D00000066773, D00000067078, D00000067079, D00000067081, D00000067082, D00000067086, D00000067088, D00000067092, D00000067094, D00000067097, D00000067099, D00000067100, D00000067103, D00000067108, D00000067109, D00000067114, D00000067117, D00000067129, D00000067133, D00000067135, D00000067136, D00000067138, D00000067139, D00000067143, D00000067145, D00000067171, D00000067172, D00000067174, D00000067178, D00000067180, D00000067183, D00000067184, D00000067186, D00000067192, D00000067195, D00000067197, D00000067199, D00000067204, D00000067209, D00000067212, D00000067217, D00000067219, D00000067224, D00000067233, D00000067235, D00000067267, D00000067303, D00000067384, D00000067456, D00000067577, D00000067601, D00000067614, D00000067638, D00000067640, D00000067644, D00000067646, D00000067651, D00000067652, D00000067653, D00000067654, D00000067655, D00000067658, D00000067660, D00000067664, D00000067665, D00000067666, D00000067667, D00000067668, D00000067669, D00000067696, D00000067697, D00000067714, D00000067748, D00000067755, D00000067756, D00000067758, D00000067762, D00000067763, D00000067764, D00000067765, D00000067769, D00000067770, D00000067771, D00000067772, D00000067773, D00000067777, D00000067785, D00000075495, D00000075574, D00000085953, D00000085968, D00000089895, D00000089936, D00000090085, D00000094487, D00000094513, D00000094806, D00000097094, D00000104028, D00000104049, D00000104062, D00000104086, D00000104174, D00000105727, D00000105728, D00000107074, D00000107083, D00000107094, D00000107112, D00000107116, D00000107180, D00000107267, D00000107378, D00000107395, D00000107405, D00000107502, D00000107507, D00000107537, D00000107565, D00000107711, D00000107713, D00000107720, D00000119052, D00000120527, D00000120550, D00000121435, D00000121441, D00000121442, D00000121455, D00000121456, D00000121457, D00000121458, D00000121459, D00000121461, D00000121462, D00000121464, D00000121465, D00000121469, D00000121470, D00000121472, D00000121476, D00000121477, D00000121482, D00000121506, D00000121527, D00000121528, D00000122755, D00000122789, D00000122794, D00000122798, D00000122806, D00000122808, D00000122813, D00000122817, D00000122845, D00000122847, D00000134901, D00000136856, D00000136864, D00000136951, D00000136957, D00000136966, D00000144818, D00000144829, D00000144830, D00000144838, D00000144848, D00000149066, D00000149085, D00000149113, D00000149120, D00000149695, D00000149701, D00000152050, D00000160405, D00000160423, D00000160496, D00000160502, D00000172568, D00000175676, D00000175713, D00000175748, D00000175769, D00000178019, D00000178021, D00000178026, D00000178029, D00000178030, D00000183047, D00000183082, D00000183146, D00000183662, D00000183746, D00000183758, D00000183759, D00000183761, D00000183775, D00000183796, D00000196083, D00000196115, D00000201889, D00000203954, D00000212126, D00000212130, D00000223042, D00000248279, D00000248281, D00000248287, D00000248288, D00000248295, D00000248296, D00000248298, D00000248316, D00000269007, D00000269308, D00000269415, D00000269625, D00000269654, D00000269743, D00000269816, D00000269852, D00000269854, D00000269855, D00000269856, D00000269858, D00000269859, D00000269864, D00000269865, D00000269867, D00000269868, D00000269869, D00000269870, D00000269871, D00000269873, D00000269875, D00000269881, D00000269882, D00000269884, D00000269887, D00000269889, D00000269890, D00000269891, D00000269893, D00000269894, D00000269896, D00000269898, D00000269900, D00000269901, D00000269902, D00000269903, D00000269904, D00000269905, D00000269906, D00000269907, D00000269910, D00000269920, D00000269926, D00000269928, D00000269931, D00000269932, D00000269933, D00000269934, D00000269935, D00000269936, D00000269937, D00000269938, D00000269939, D00000269940, D00000269941, D00000269942, D00000269943, D00000269944, D00000269946, D00000269947, D00000269949, D00000269950, D00000269951, D00000269952, D00000269953, D00000269954, D00000269955, D00000269956, D00000269957, D00000269958, D00000269959, D00000269960, D00000269961, D00000269962, D00000269963, D00000269964, D00000269965, D00000269966, D00000269967, D00000269968, D00000269969, D00000269970, D00000269971, D00000269972, D00000269973, D00000269974, D00000269975, D00000269976, D00000269977, D00000269978, D00000269979, D00000269980, D00000269981, D00000269982, D00000269983, D00000269984, D00000269985, D00000269986, D00000269987, D00000269988, D00000269989, D00000269990, D00000269991, D00000269992, D00000269993, D00000269994, D00000269995, D00000269996, D00000269997, D00000269998, D00000269999, D00000270000, D00000270001, D00000270002, D00000270003, D00000270004, D00000270005, D00000270006, D00000270007, D00000270008, D00000270009, D00000270010, D00000270011, D00000270012, D00000270013, D00000270014, D00000270015, D00000270016, D00000270017, D00000270018, D00000270019, D00000270020, D00000270021, D00000270022, D00000270023, D00000270024, D00000270025, D00000270026, D00000270028, D00000270029, D00000270031, D00000270032, D00000270033, D00000270034, D00000270035, D00000270036, D00000270037, D00000270038, D00000270040, D00000270041, D00000270042, D00000270043, D00000270044, D00000270045, D00000270046, D00000270047, D00000270048, D00000270049, D00000270050, D00000270051, D00000270052, D00000270053, D00000270054, D00000270055, D00000270056, D00000270058, D00000270059, D00000270060, D00000270061, D00000270062, D00000270063, D00000270064, D00000270065, D00000270067, D00000270068, D00000270069, D00000270070, D00000270071, D00000270072, D00000270073, D00000270074, D00000270075, D00000270076, D00000270077, D00000270078, D00000270079, D00000270080, D00000270081, D00000270082, D00000270084, D00000270085, D00000270086, D00000270088, D00000270089, D00000270090, D00000270091, D00000270092, D00000270093, D00000270094, D00000270095, D00000270096, D00000270097, D00000270098, D00000270099, D00000270100, D00000270101, D00000270102, D00000270103, D00000270104, D00000270105, D00000270106, D000 …
Show 2 more code fieldsShow fewer
What the firm is doing
On February 13, 2025, URGENT: MEDICAL DEVICE CORRECTION letters were sent to customers. REQUIRED ACTIONS Customers who have AEDs should routinely: (1) Monitor device for self-test results. (2) For customers who experience a self-test failure, take action to resolve any alerts as soon as possible. Customers who have at-risk devices should immediately: (1) Communicate this notification to G5 AED users. (2) Ensure users have a program in place that periodically monitors the status of these devices, in accordance with G5 User s Guide. (3) EC 501 is likely due to exposure to humidity outside the device s published specification. Ensure devices are stored within the device s published specifications: " Temperature: 0C to 50C (32F to 122F) " Humidity: 10% to 95% (non-condensing) (4) Respond to ZOLL via the customer notification form acknowledging that you have received this notice. We have notified the appropriate regulatory agencies of this correction and expect it to be classified as a recall. We apologize for any inconvenience this may cause you and thank you in advance for assistance in implementing this correction. Ensuring these devices are rescue ready is our highest priority. Our 24/7 technical support numbers 1 (800) 348-9011 or 1 (978) 421-9460 and are available to assist users with any aspect of this notice. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA s MedWatch Adverse Event Reporting program either online, by regular mail or by fax with the fax number being 1-800-FDA-0178.
DistributionShow detailsHide
Domestic: Nationwide Distribution International: AE, AI, AM, AR, AT, AU, BD, BE, BG, BH, BM, BN, BS, CA, CH, CL, CN, CO, CR, CZ, DE, DK, DO, EG, ES, FI, FR, GB, GH, GU, HK, HR, HU, ID, IE, IL, IN, IS, IT, JE, JM, JP, KR, KW, KZ, LB, LT, MA, MC, MD, ME, MQ, MS, MT, MX, MY, NC, NG, NL, NO, NZ, OM, PA, PE, PG, PH, PK, PL, PR, PT, QA, RE, RO, RS, RU, SA, SE, SG, SI, SK, SM, TC, TH, TN, TR, TW, UA, US, VG, ZA.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-1319-2025
- FDA device classification · MKJOfficial FDA classification for this device type
- CFR regulation · 21 CFR 870.5310The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find ZOLL Medical CorporationSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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